Canonical Allele Identifier: CA2636259553
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v4: 17-15999750-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999750C>A , CM000679.2:g.15999750C>A GRCh38
NC_000017.10:g.15903064C>A , CM000679.1:g.15903064C>A GRCh37
NC_000017.9:g.15843789C>A NCBI36
NG_029806.1:g.5371C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-99C>A ENSP00000261647.5:n.-99C>A
NM_001271420.1:c.-557C>A NP_001258349.1:n.-557C>A
NM_017775.3:c.-99C>A NP_060245.3:n.-99C>A
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